ライフサイエンスコーパス: intestinalis

1 (Faecalibacterium prausnitzii and Roseburia intestinalis).

2 tochord-specific CRM from the ascidian Ciona intestinalis.

3 ssion patterns of NCLC in the ascidian Ciona intestinalis.

4 cardiac cell migration in the ascidian Ciona intestinalis.

5 ignyi to its divergent sister species, Ciona intestinalis.

6 performed by using the basal chordate Ciona intestinalis.

7 om another deep-branching eukaryote, Giardia intestinalis.

8 rong conservation between C. savignyi and C. intestinalis.

9 a of a sibling chordate, the ascidian, Ciona intestinalis.

10 nce between northern European and Pacific C. intestinalis.

11 Encephalitozoon hellem, and Encephalitozoon intestinalis.

12 Enterocytozoon bieneusi and Encephalitozoon intestinalis.

13 n the genome sequences of the ascidian Ciona intestinalis.

14 ns in the ascidians Ciona savignyi and Ciona intestinalis.

15 sue-specific enhancers in the ascidian Ciona intestinalis.

16 e genome of the most studied ascidian, Ciona intestinalis.

17 rosophila melanogaster, zebrafish, and Ciona intestinalis.

18 CiVegTR, was isolated in the ascidian Ciona intestinalis.

19 ae, cysts, and a few trophozoites of Giardia intestinalis.

20 s-reactivity to spores of E. cuniculi and E. intestinalis.

21 infections of Enterocytozoon bieneusi and E. intestinalis.

22 rstanding of the pathogenesis of pneumatosis intestinalis.

23 Encephalitozoon cuniculi, E. hellem, and E. intestinalis.

24 li, E. hellem, and Encephalitozoon (Septata) intestinalis.

25 been identified as the anaerobic Bacteroides intestinalis.

26 aining three were more closely related to F. intestinalis.

27 caceae, along with exogenously introduced B. intestinalis.

28 ting microsporidian species, Encephalitozoon intestinalis.

29 system of the ascidian tadpole larva, Ciona intestinalis.

30 oides strains increased, most prominently B. intestinalis.

31 to ferment arabinoxylans include Bacteroides intestinalis.

32 e closure in the invertebrate chordate Ciona intestinalis.

33 amics using the invertebrate chordate, Ciona intestinalis.

34 ism for zippering in a basal chordate, Ciona intestinalis.

35 in the study group in favour of pneumatosis intestinalis.

36 CNS of a simple chordate, the ascidian Ciona intestinalis.

37 breaks in the genome of the sea squirt Ciona intestinalis.

38 y >110% for C.milii and from 20 to 40% for C.intestinalis.

39 reases with whey, but is not repressed in C. intestinalis.

40 velopment of the invertebrate chordate Ciona intestinalis.

41 f gastrulation to swimming tadpoles-in Ciona intestinalis.

42 o investigate cilia in the urochordate Ciona intestinalis.

43 network in the invertebrate chordate, Ciona intestinalis.

44 ectodermal development in the ascidian Ciona intestinalis.

45 s in different nematodes and the chordate C. intestinalis.

46 histolytica or E dispar (0.61, 0.38-0.99), G intestinalis (0.63, 0.50-0.80), and Cryptosporidium spp

47 spar (OR 0.56, 95% CI 0.42-0.74) and Giardia intestinalis (0.64, 0.51-0.81), but not for Blastocystis

48 Complete sequences from Encephalitozoon intestinalis (2.3 Mbp) and Encephalitozoon cuniculi (2.9

49 Here, we show that GiKIN14a from Giardia intestinalis [2] is an unconventional Ncd-type kinesin-1

50 43 (45.8%) were positive for Encephalitozoon intestinalis, 2 (2.1%) were positive for Encephalitozoon

51 olescents, 22 of whom were diagnosed with G. intestinalis, 53 with E. histolytica and/or E. dispar, a

52 Giardia intestinalis, a human intestinal parasite and member of

53 and snail homologues in the ascidian, Ciona intestinalis, a member of the subphylum Urochordata, the

54 have examined ASICs from the ascidian Ciona intestinalis, a simple chordate organism whose nervous s

55 sed foods, selectively increases Collinsella intestinalis absolute abundance and induces Collinsella

56 he P. aeruginosa, E. coli, B. mallei, and G. intestinalis ADIs.

57 The incidence of pneumatosis intestinalis after lung transplantation in our center wa

58 rogenitor cells of the simple chordate Ciona intestinalis also generate precursors of the atrial siph

59 Expression of Ciona intestinalis alternative oxidase (AOX) in mitochondrial

60 e was rescued by ectopic expression of Ciona intestinalis alternative oxidase (AOX)(12), which also o

61 erevisiae NADH dehydrogenase (NDI1) or Ciona intestinalis alternative oxidase, which can complement t

62 he ARNTL gene family in the genomes of Ciona intestinalis, amphioxus, zebrafish, and human.

63 brafish (Danio rerio) and the ascidian Ciona intestinalis, an invertebrate chordate belonging to the

64 egulatory factor (MRF) of the ascidian Ciona intestinalis, an invertebrate chordate.

65 ressed by the human gut bacteria Bacteroides intestinalis and Bacteroides ovatus grown in monoculture

66 on of TERT genes from two sea squirts, Ciona intestinalis and Ciona savignyi.

67 ly gene was identified in the ascidian Ciona intestinalis and designated CiMDF (Ciona intestinalis Mu

68 organisms that make cellulose, such as Ciona intestinalis and Dictyostelium discoideum, revealed the

69 the genomes of Encephalitozoon cuniculi, E. intestinalis and E. bieneusi.

70 One patient was infected with both E. intestinalis and E. cuniculi.

71 lytica and/or E. dispar, and 14 with both G. intestinalis and E. histolytica and/or E. dispar.

72 Pneumatosis intestinalis and free air had 100% (four of four control

73 of the order of approximately 20% for the C.intestinalis and H.sapiens assemblies, which is signific

74 Using AAA mice, we show that R. intestinalis and its metabolite butyrate significantly r

75 e two native species of Lactobaccillacea: L. intestinalis and L. murinus.

76 lycolytic pathway of the diplomonads Giardia intestinalis and Spironucleus barkhanus, Type I amitocho

77 rosophila melanogaster, Daphnia pulex, Ciona intestinalis and Strongylocentrotus purpuratus.

78 pharyngeal epithelium of the ascidian Ciona intestinalis and the amphioxus Branchiostoma lanceolatum

79 ue and Opossum, the chordate genome of Ciona intestinalis and the import and integration of the yeast

80 nt from the genomes of the urochordate Ciona intestinalis and the lower eukaryotes D. melanogaster an

81 a simple method to introduce DNA into Ciona intestinalis and the several available tissue-specific p

82 We identified putative MBL homologs in Ciona intestinalis and Trichoplax adhaerens, and investigated

83 to 7.8 x 10(4) (mean, 1.5 x 10(4)/ml) for E. intestinalis, and 1.8 x 10(2) to 3.6 x 10(2) for E. hell

84 AG:754, Parabacterium johnsonii, Bacteroides intestinalis, and Bifidobacterium breve were significant

85 multaneous identification of E. bieneusi, E. intestinalis, and E. hellem, as well as Encephalitozoon

86 med, non-operative management of pneumatosis intestinalis, and potentially gas gangrene is becoming m

87 al gut bacteria, exemplified by increased R. intestinalis, and reduction of mucus-degraders.

88 Encephalitozoon cuniculi or Encephalitozoon intestinalis, and the recruitment of naive monocytes was

89 expressed an alternative oxidase from Ciona intestinalis (AOX) in ETC-deficient murine RPE in vivo t

90 nensis, Enterocytozoon bieneusi, and Septata intestinalis are intestinal spore-forming protozoa that

91 Encephalitozoon cuniculi and Encephalitozoon intestinalis are preferentially recognized by TLR2 and n

92 rchers identify butyrate-producing Roseburia intestinalis as a mediator of pain sensitivity along the

93 hese findings highlight the usefulness of C. intestinalis as a model organism for investigating vitam

94 notochord of the invertebrate chordate Ciona intestinalis as a model.

95 Using Ciona intestinalis as a simple chordate model, we show that bi

96 hylogenetic position of the sea squirt Ciona intestinalis as part of the sister group to the vertebra

97 to low grazer affinity for macroalgae (Ulva intestinalis), as recruitment of both macroalgae and dia

98 rom 3 of 7 ASF species (ASF360 Lactobacillus intestinalis, ASF361 Ligilactobacillus murinus, and ASF5

99 For C. intestinalis, Bayesian analysis suggested a natural amph

100 ing basis of enhancer activity for the Ciona intestinalis betagamma-crystallin gene, which drives exp

101 317, Eisenbergiella massiliensis, Sellimonas intestinalis, Blautia wexlerae, and Alistipes shahii).

102 In ascidians, such as Ciona intestinalis, Brachyury is expressed exclusively in the

103 The presence of E. intestinalis but not Encephalitozoon hellem or Encephali

104 uently identified in human, mouse, and Ciona intestinalis, but their existence in dinoflagellates rem

105 iens, Mus musculus, Takifugu rubripes, Ciona intestinalis, Caenorhabditis elegans, Drosophila melanog

106 rointestinal disease whereas Encephalitozoon intestinalis causes both a disseminated and an intestina

107 wer substitutions than the sea squirt (Ciona intestinalis) CB1 sequence.

108 rhabditis elegans (Ce), the sea squirt Ciona intestinalis (Ci) and amphioxus Branchiostoma floridae (

109 MRF gene of the invertebrate chordate Ciona intestinalis (Ci-MRF).

110 tage sensor of the prototypic VSP from Ciona intestinalis, Ci-VSP, we generated chimeric proteins tha

111 recently identified in the urochordate Ciona intestinalis (CiCBR).

112 The C. intestinalis cilia have a 9+0 ring ultrastructure, howev

113 A chordate ortholog of UNC-3, Ciona intestinalis COE, was also both required and sufficient

114 ous epithelium is replaced by specialised or intestinalised columnar epithelium.

115 The ascidian Ciona intestinalis, commonly known as a 'sea squirt', has beco

116 Here we show that the gut mucosa of Ciona intestinalis contains an extensive matrix of chitin fibr

117 The diplomonad parasite Giardia intestinalis contains two functionally equivalent nuclei

118 responses to eight enteropathogens (Giardia intestinalis, Cryptosporidium parvum, Entamoeba histolyt

119 nfection with the protozoan parasite Giardia intestinalis decreases diarrhoeal severity.

120 We track E. intestinalis development through its life cycle, which a

121 onse in primary human macrophages and the E. intestinalis developmental program.

122 nome of a urochordate, the sea squirt, Ciona intestinalis, did not turn up any genuine orthologs for

123 Sequence analysis of the C. intestinalis Dll-A-B cluster reveals a 378bp region upst

124 High levels of Bacteroides intestinalis DNA could also be detected in this cat's fe

125 Abundances of Faecalibacillus intestinalis, Dorea formicigenerans, Ruminococcus torque

126 cluster encoded on the genome of Bacteroides intestinalis DSM 17393.

127 tiation of three Encephalitozoon species (E. intestinalis, E. cuniculi, and E. hellem).

128 DNA encoding APS reductase from Enteromorpha intestinalis (EAPR) was cloned by functional complementa

129 lylsulfate (APS) reductase from Enteromorpha intestinalis (EiAPR) is composed of two domains that fun

130 improve and enrich the description of Ciona intestinalis embryonic development, based on an improved

131 Comprehensive gene networks in Ciona intestinalis embryos provide a foundation for characteri

132 d cell lineage of the pigment cells in Ciona intestinalis embryos.

133 es included Cyclospora cayetanensis, Giardia intestinalis, Entamoeba coli, Iodamoeba butschlii, Endol

134 The E. intestinalis enzyme (EiAPR) is composed of a reductase d

135 Here we show that the tunicate Ciona intestinalis exhibits a proto-placodal ectoderm (PPE) th

136 Our data show that Encephalitozoon intestinalis exploits sulfated glycans such as the cell

137 inent butyrate-producing Firmicute Roseburia intestinalis expresses two loci conferring metabolism of

138 of the primitive monolobal transferrin of C. intestinalis for comparison with higher order bilobal tr

139 gene families to examine the tunicate Ciona intestinalis for evidence of structures homologous to ve

140 e caused by the unicellular parasite Giardia intestinalis, for which metronidazole is the main treatm

141 (formerly Ciona intestinalis type A) and C. intestinalis (formerly Ciona intestinalis type B), globa

142 ng demand for diagnostic testing for Giardia intestinalis (G. lamblia) and Cryptosporidium parvum, wi

143 ountries, including Giardia lamblia (syn. G. intestinalis/G. duodenalis) and Cryptosporidium spp., us

144 ing for a direct orthology between the Ciona intestinalis gene CiPax6 and Pax6 in mammals.

145 We surveyed the ongoing G. intestinalis genome project data and have identified, ve

146 distribution of DNA methylation in the Ciona intestinalis genome.

147 e been sequenced since the release of the C. intestinalis genome.

148 nsive necrotizing enterocolitis (pneumatosis intestinalis), gestational age of less than 25 weeks, an

149 Giardia intestinalis, Giardia duodenalis) is an enteric protozoa

150 G. intestinalis GK expressed in Escherichia coli was specif

151 ing SG degradation by individual purified B. intestinalis glycoside hydrolases.

152 x-binding protein (TBP) homolog from Giardia intestinalis (gTBP) is highly divergent, lacking key phe

153 timated that the invertebrate chordate Ciona intestinalis has 15,500 protein-coding genes (+/-3,700).

154 The ascidian Ciona intestinalis has a monolobal transferrin (nicatransferri

155 ive epidermal transcription suggests that C. intestinalis has arthropod-like Hox patterning in the ep

156 Genomic Southern blots showed that C. intestinalis has only one MyoD family gene, suggesting t

157 In spite of this, not many isolates of E. intestinalis have been established in culture.

158 , we provide an organismal perspective of C. intestinalis, highlighting aspects of its life history a

159 n development and that in the tunicate Ciona intestinalis, Hmx is necessary and sufficient to drive t

160 forward genetic screen in the ascidian Ciona intestinalis identified a mutant line (frimousse) with a

161 edge, this is the first identification of E. intestinalis in animals other than humans.

162 Encephalitozoon cuniculi and Encephalitozoon intestinalis in both form and content.

163 poridium, Entamoeba histolytica, and Giardia intestinalis in children.

164 istinguishing E. cuniculi, E. hellem, and E. intestinalis in clinical specimens.

165 the preference of B. thetaiotaomicron and B. intestinalis in FVP degradation.

166 Pneumatosis intestinalis in lung transplant patients is a rare compl

167 ignificantly higher abundance of Bacteroides intestinalis in patients with toxicity, with upregulatio

168 of an introduced marine invertebrate (Ciona intestinalis) in Northern California.

169 The higher prevalence of Encephalitozoon intestinalis, in 21 (12.8%) patients, than of Enterocyto

170 AZT also showed a good effect in G. intestinalis-infected gerbils, reducing both the number

171 shown herein suggest the possibility that E. intestinalis infection may be zoonotic in origin.

172 in both the parasite and the host during E. intestinalis infection of human macrophages in vitro.

173 network is substantially remodeled during E. intestinalis infection, leading to mitochondrial fragmen

174 native for the specific identification of E. intestinalis infections.

175 The binucleate pathogen Giardia intestinalis is a highly divergent eukaryote with a semi

176 Encephalitozoon intestinalis is a microsporidian species that infects th

177 Encephalitozoon intestinalis is a prevalent human-infecting species that

178 Our findings highlight that R. intestinalis is a primary degrader of this dietary fiber

179 Pneumatosis intestinalis is a radiological finding characterized by

180 Giardia intestinalis is a significant cause of diarrheal disease

181 The invertebrate chordate Ciona intestinalis is a widely used model organism in biologic

182 ification in the invertebrate chordate Ciona intestinalis is similar to that of vertebrates but only

183 Giardia intestinalis is the most commonly reported human intesti

184 Encephalitozoon intestinalis (Septata intestinalis) is the second most prevalent microsporidia

185 dence that the embryo of the ascidian, Ciona intestinalis, is an easily manipulated system for invest

186 While our experiments focused on B. intestinalis, it is likely that the extracellular enzyme

187 lia may have a role in the development of C. intestinalis left-right asymmetry but that this would ha

188 tes including Entamoeba histolytica, Giardia intestinalis, Leishmania spp., Plasmodium spp., Toxoplas

189 In Ciona intestinalis, leprecan was identified as a target of the

190 Pneumatosis cystoides intestinalis may be due to excessive hydrogen production

191 Finally, gut bacteria Lactobacillus intestinalis metabolized VA and specifically restored RA

192 nstrate that, in the chordate ascidian Ciona intestinalis, miR-124 plays an extensive role in promoti

193 ona intestinalis and designated CiMDF (Ciona intestinalis Muscle Determination Factor).

194 ugh mediation of Ca(2+) transients, in Ciona intestinalis neural induction.

195 ntinuous cultivation of eight isolates of E. intestinalis obtained from different samples including t

196 Moreover, recent phylogenies reveal that C. intestinalis occupies a privileged branch in the tree of

197 extracts from the common green seaweed Ulva intestinalis on germination and root development in the

198 growth of the colonic bacterium Bacteroides intestinalis on wheat arabinoxylan.

199 Bacteroidetes members, including Bacteroides intestinalis, on complex arabinoxylans results in accumu

200 Single application of Roseburia intestinalis or Anaerostipes caccae was even more effect

201 the treatment of diarrhea caused by Giardia intestinalis or Entamoeba histolytica and/or E. dispar i

202 Pneumatosis cystoides intestinalis (PCI) is a rare disorder characterized by t

203 wel ischemia (free air or fluid, pneumatosis intestinalis, portal venous gas, mesenteric stranding) w

204 Larvae of the tunicate Ciona intestinalis possess a central nervous system of 177 neu

205 Here we show that the tunicate Ciona intestinalis possesses a cephalic melanocyte lineage (a9

206 te this process in the simple chordate Ciona intestinalis Previous studies have implicated Nodal and

207 ynthesis in the green macroalga Enteromorpha intestinalis proceeds by a route entirely distinct from

208 k ventral cells, TVCs) of the ascidian Ciona intestinalis provide a simple chordate model with which

209 S of the tadpole larva of the ascidian Ciona intestinalis provides us with a chordate nervous system

210 e gene for the FlgCK from the tunicate Ciona intestinalis, providing support for the linkage of the p

211 cellular eukaryotes, the diplomonads Giardia intestinalis (published earlier) and Spironucleus barkha

212 d even a highly divergent invertebrate Ciona intestinalis qualitatively and quantitatively suppressed

213 d by a common human gut commensal, Roseburia intestinalis (R. int), and T and B cell autoepitopes in

214 on simulated next-generation data from Ciona intestinalis, real next-generation data from Drosophila

215 Antibodies from mice infected with E. intestinalis recognized SWP1 and SWP2.

216 prausnitzii, Bacteroides vulgatus, Roseburia intestinalis, Ruminococcus obeum, Salmonella typhimurium

217 Encephalitozoon intestinalis (Septata intestinalis) is the second most p

218 t rabbit anti-E. cuniculi and rabbit anti-E. intestinalis sera were reactive with homologous spores o

219 icroscopy, using a polyclonal rabbit anti-E. intestinalis serum at a dilution of 1:400.

220 In mixed cultures, R. intestinalis shares the available beta-mannan with Bacte

221 ted by our experiments in the ascidian Ciona intestinalis showing that the peripheral sensory neurons

222 In the ascidian, Ciona intestinalis, snail (Ci-sna) is expressed at the 32-cell

223 of two cryptic species within the present C. intestinalis species.

224 These data show that E. intestinalis specifically adheres to target cells by way

225 A large number of C. intestinalis specimens were collected from four continen

226 as inhibitors in spore adherence assays, E. intestinalis spore adherence is reduced by as much as 88

227 In studies, as few 10 to 50 Encephalitozoon intestinalis spores could be detected when seeded in a 1

228 ulfated glycans are used, suggesting that E. intestinalis spores utilize sulfated host cell glycans i

229 les (9.6%) contained both E. bieneusi and E. intestinalis spores.

230 fecal specimens spiked with Encephalitozoon intestinalis spores.

231 esced brightly, indicating that they were E. intestinalis spores.

232 al focal intramural gas bubbles (pneumatosis intestinalis) surrounding the polypectomy site.

233 Diplomonads including Giardia intestinalis (syn.

234 Giardia intestinalis (syn. lamblia) is one of the most widesprea

235 moto- and interneuron subtypes in the Ciona intestinalis tadpole larva.

236 the rhythmic swimming behavior of the Ciona intestinalis tadpole.

237 The C. intestinalis TERT (CinTERT) gene encodes 907 amino acids

238 eral cDNAs derived from the sea squirt Ciona intestinalis that encode vitamin K-dependent proteins.

239 Some individuals harbour Bacteroides intestinalis that is incapable of consuming polymeric xa

240 ed short-tailed mutant in the ascidian Ciona intestinalis that is the product of a premature stop in

241 fied in the primitive ascidian species Ciona intestinalis that possesses the characteristic features

242 stomian invertebrate - the urochordate Ciona intestinalis - that is orthologous to vertebrate cannabi

243 Encephalitozoon (Septata) intestinalis, the agent that causes a disseminated infec

244 e in the tadpole larva of the tunicate Ciona intestinalis, the bipolar tail neuron, shares a set of f

245 In the simple chordate Ciona intestinalis, the notochord plate consists of just 40 ce

246 In Ciona intestinalis, the palps consist of three conical protrus

247 Here, we characterized the G. intestinalis thymidine kinase, a divergent member of the

248 e, we employ the invertebrate chordate Ciona intestinalis to delineate an essential in vivo role for

249 gical simplicity of the basal chordate Ciona intestinalis to elucidate Mesp regulation and function.

250 ild populations of the marine chordate Ciona intestinalis to show that levels of buffering are matern

251 nipulability, we chose the sea squirt, Ciona intestinalis, to explore intraspecies sequence compariso

252 nd streamlined genome of the ascidian, Ciona intestinalis, to investigate heart development in a basa

253 of noncoding elements, which we showed in C. intestinalis transgenic assays to act as tissue-specific

254 nst WT as well as metronidazole-resistant G. intestinalis trophozoites.

255 ive tunicates, Ciona robusta (formerly Ciona intestinalis type A) and C. intestinalis (formerly Ciona

256 type A) and C. intestinalis (formerly Ciona intestinalis type B), globally distributed and sympatric

257 .3 Mb for the microsporidian Encephalitozoon intestinalis up to 8000 Mb for Entomophaga aulicae, with

258 e marine macrophytic green alga Enteromorpha intestinalis uses reduced glutathione as the electron do

259 ron microscopy reconstruction of Bacteroides intestinalis virus PhicrAss001(6), providing the structu

260 The Ciona intestinalis voltage-sensing phosphatase (Ci-VSP) is a m

261 d the sensitivity of Kv7.5 channels to Ciona intestinalis voltage-sensing phosphatase (Ci-VSP)-induce

262 ts suggest that the native S4 from the Ciona intestinalis voltage-sensitive phosphatase (Ci-VSP) does

263 The Ciona intestinalis voltage-sensitive phosphatase (Ci-VSP) repr

264 ge-sensing membrane proteins using the Ciona intestinalis voltage-sensitive phosphatase (CiVSP).

265 sists of the voltage-sensing domain of Ciona intestinalis voltage-sensitive phosphatase and super ecl

266 channel and the voltage sensor of the Ciona intestinalis voltage-sensitive phosphatase, against expe

267 are significantly faster than those of Ciona intestinalis voltage-sensitive phosphatase.

268 he genome of the invertebrate chordate Ciona intestinalis was found to be a stable mosaic of methylat

269 A search of patients with pneumatosis intestinalis was performed in the database of the Lung T

270 Specifically, R. intestinalis was significantly reduced in AAA patients.

271 tern of CiMDF, the MyoD-family gene of Ciona intestinalis, was analyzed in unmanipulated and microsur

272 raft genome of the primitive chordate, Ciona intestinalis, was published three years ago.

273 ents from the microsporidian Encephalitozoon intestinalis were characterized.

274 ed proton channels in humans, mice and Ciona intestinalis were discovered.

275 ichia coli, Burkholderia mallei, and Giardia intestinalis were examined in order to demonstrate the g

276 anscribed in eggs of Xenopus laevis or Ciona intestinalis were found, pinpointing evolutionary conser

277 Eggs of the ascidian Ciona intestinalis were injected with the Src-homology 2 domai

278 cant associations with E. histolytica and G. intestinalis were not found.

279 Encephalitozoon hellem, E. cuniculi, and E. intestinalis were propagated in axenic cultures of monke

280 ter and in the non-vertebrate chordate Ciona intestinalis, which each have only one talin gene, alter

281 arison of talins in the model urochordate C. intestinalis, which has one talin gene that produces two

282 We show that the urochordate Ciona intestinalis, which split from the vertebrate lineage be

283 CE2 and RiCE17, from the Firmicute Roseburia intestinalis, which together deacetylate complex galacto

284 icroscopy to observe trophozoites of Giardia intestinalis, which were labeled with an amino-specific

285 acterization of two immunogenic SWPs from E. intestinalis will allow the study of exospore structure

286 that occasionally the origin of pneumatosis intestinalis will remain cryptogenic--caused but unexpla

287 the human-infecting species, Encephalitozoon intestinalis, within host cells.

288 fied ABC proteins from the sea squirt (Ciona intestinalis), zebrafish (Danio rerio), and chicken (Gal